Alcohol does not impact chronic hepatitis C treatment outcomes but increases risk for progressive liver disease: Findings from a prospective multicentre Australian study (OPERA‐C)

Author:

Clark Paul J.12,Valery Patricia C.23ORCID,Strasser Simone I.4,Weltman Martin5,Thompson Alex6,Levy Miriam T.7,Leggett Barbara28,Zekry Amany9,Rong Julian10,Sinclair Marie11,George Jacob1213,Sievert William14,MacQuillan Gerry15,Tse Edmund16,Nicoll Amanda17,Wade Amanda1819,Cheng Wendy20,Roberts Stuart K.21

Affiliation:

1. Department of Gastroenterology, Alcohol and Drug Assessment Unit Princess Alexandra and Mater Hospitals Brisbane Australia

2. Faculty of Medicine The University of Queensland Brisbane Australia

3. QIMR Berghofer Medical Research Institute Brisbane Australia

4. AW Morrow Gastroenterology and Liver Centre Royal Prince Alfred Hospital Sydney Australia

5. Hepatology Services Nepean Hospital Sydney Australia

6. Department of Gastroenterology St Vincent's Hospital Melbourne Australia

7. Department of Gastroenterology and Liver Liverpool Hospital Sydney Australia

8. Department of Gastroenterology and Hepatology Royal Brisbane and Women's Hospital Brisbane Australia

9. Department of Gastroenterology and Hepatology St George Hospital Sydney Australia

10. Gippsland Gastroenterology Latrobe Regional Hospital Traralgon Australia

11. Department of Gastroenterology and Hepatology Austin Hospital Melbourne Australia

12. Faculty of Medicine The University of Sydney Sydney Australia

13. Storr Liver Centre Westmead Hospital Sydney Australia

14. Gastrointestinal and Liver Unit Monash Health and Monash University Melbourne Australia

15. Department of Hepatology and Liver Transplant Unit Sir Charles Gairdner Hospital Perth Australia

16. Hepatology, Royal Adelaide Hospital Adelaide Australia

17. Eastern Health Melbourne Australia

18. Burnet Institute Melbourne Australia

19. Barwon Health Liver Clinic University Hospital Geelong Australia

20. Department of Gastroenterology & Hepatology Royal Perth Hospital Perth Australia

21. The Alfred Hospital and Monash University CCS Melbourne Australia

Abstract

AbstractIntroductionAlcohol use is common in patients with chronic hepatitis C virus (HCV) infection. We examined the impact of alcohol use on direct‐acting antiviral (DAA) therapy outcome and the clinical course of liver disease and 2‐year survival for patients receiving HCV DAA therapy.MethodsAdults (n = 2624) recruited from 26 Australian hospital liver clinics during 2016–2021 were followed up for 2 years. Risky alcohol use was defined by a combination of self‐report (≥40 g/day of ethanol), physician‐reported history of problematic alcohol use, and anti‐craving medication prescription via population‐based database linkage. We examined factors associated with advanced liver fibrosis and survival using multivariable logistic and Cox regression.ResultsAmong 1634 patients (62.3%) with risky alcohol use, 24.6% reported consuming ≥40 g/day of alcohol, 98.3% physician‐reported problematic alcohol use; only 4.1% were dispensed naltrexone/acamprosate. One hundred and forty‐three patients with cirrhosis reported ≥40 g/day of alcohol, 6 (4.3%) were prescribed naltrexone/acamprosate. Risky alcohol use was associated with advanced fibrosis (adjusted‐odds ratio 1.69, 95% confidence interval 1.32–2.17) and patients were over‐represented for cirrhosis (45.1% vs. 25.6% in no‐risky alcohol use [p < 0.001]) and hepatocellular carcinoma (5.7% vs. 2.5% [p < 0.001]). Sustained viral response (p = 0.319) and 2‐year survival (adjusted‐hazard ratio 1.98, 95% confidence interval 0.84–4.63) after DAA therapy were not associated with risky alcohol use.Discussion and ConclusionsRisky alcohol use in HCV patients was prevalent, but did not reduce HCV cure. Treatment for alcohol dependence was low. Risky alcohol use may be under‐recognised in liver clinics. Better integration of addiction medicine into liver services and increased resourcing and addiction medicine training opportunities for hepatologists may help address this.

Funder

Gastroenterological Society of Australia

Gilead Sciences

Merck

AbbVie

National Health and Medical Research Council

Publisher

Wiley

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